clonidine hydrochloride

Generic: clonidine hydrochloride

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clonidine hydrochloride
Generic Name clonidine hydrochloride
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clonidine hydrochloride .3 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-056
Product ID 62332-056_100955f8-68c5-437e-9710-8546164e8735
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091368
Listing Expiration 2026-12-31
Marketing Start 2016-05-03

Pharmacologic Class

Classes
adrenergic alpha2-agonists [moa] central alpha-2 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332056
Hyphenated Format 62332-056

Supplemental Identifiers

RxCUI
884173 884185 884189
UPC
0362332056309 0362332054305 0362332055302
UNII
W76I6XXF06

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name clonidine hydrochloride (source: ndc)
Generic Name clonidine hydrochloride (source: ndc)
Application Number ANDA091368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .3 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 CARTON (62332-056-10)
  • 30 TABLET in 1 BOTTLE (62332-056-30)
  • 100 TABLET in 1 BOTTLE (62332-056-31)
  • 500 TABLET in 1 BOTTLE (62332-056-71)
  • 1000 TABLET in 1 BOTTLE (62332-056-91)
source: ndc

Packages (5)

62332-056-10 100 TABLET in 1 CARTON (62332-056-10) 62332-056-30 30 TABLET in 1 BOTTLE (62332-056-30) 62332-056-31 100 TABLET in 1 BOTTLE (62332-056-31) 62332-056-71 500 TABLET in 1 BOTTLE (62332-056-71) 62332-056-91 1000 TABLET in 1 BOTTLE (62332-056-91)

Ingredients (1)

clonidine hydrochloride (.3 mg/1)

Linked Drug Pages (1)

clonidine hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "100955f8-68c5-437e-9710-8546164e8735", "openfda": {"upc": ["0362332056309", "0362332054305", "0362332055302"], "unii": ["W76I6XXF06"], "rxcui": ["884173", "884185", "884189"], "spl_set_id": ["61b56917-1442-4068-86d8-0e5a5a59e612"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CARTON (62332-056-10)", "package_ndc": "62332-056-10", "marketing_start_date": "20160503"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-056-30)", "package_ndc": "62332-056-30", "marketing_start_date": "20160503"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62332-056-31)", "package_ndc": "62332-056-31", "marketing_start_date": "20160503"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62332-056-71)", "package_ndc": "62332-056-71", "marketing_start_date": "20160503"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-056-91)", "package_ndc": "62332-056-91", "marketing_start_date": "20160503"}], "brand_name": "clonidine hydrochloride", "product_id": "62332-056_100955f8-68c5-437e-9710-8546164e8735", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "62332-056", "generic_name": "Clonidine Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "clonidine hydrochloride", "active_ingredients": [{"name": "CLONIDINE HYDROCHLORIDE", "strength": ".3 mg/1"}], "application_number": "ANDA091368", "marketing_category": "ANDA", "marketing_start_date": "20160503", "listing_expiration_date": "20261231"}